Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

بواسطة Maurer-Stroh, Sebastian, Soler, V. J., Tran-Viet, K.-N., Galiacy, S. D., Limviphuvadh, V., Klemm, T. P., St Germain, E., Fournie, P. R., Guillaud, C., Hawthorne, F., Suarez, C., Kantelip, B., Afshari, N. A., Creveaux, I., Luo, X., Meng, W., Calvas, P., Cassagne, M., Arne, J.-L., Malecaze, F., Young, T. L., Rozen, Steve G.
منشور في 2013

Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

بواسطة Soler, V.J., Tran-Viet, K.-N., Galiacy, S.D., Limviphuvadh, V., Klemm, T.P., St Germain, E., Fournié, P.R., Guillaud, C., Maurer-Stroh, S., Hawthorne, F., Suarez, C., Kantelip, B., Afshari, N.A., Creveaux, I., Luo, X., Meng, W., Calvas, P., Cassagne, M., Arné, J.-L., Rozen, S.G., Malecaze, F., Young, T.L.
منشور في 2014